| 1 | CDH3, EEM
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| Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).
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| Kjaer KW, Hansen L, Schwabe GC, Marques-de-Faria AP, Eiberg H, Mundlos S, Tommerup N, Rosenberg T.
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| J Med Genet 42(4):292-8. 2005
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| 2 | EEM
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| Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings.
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| Senecky Y, Halpern GJ, Inbar D, Attias J, Shohat M.
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| Am. J. Med. Genet. 101: 195-197. 2001
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| 3 | EEM
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| Alopecia, macular degeneration, and growth retardation: a new syndrome?
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| Kuster W, Majewski F, Hammerstein W.
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| Am J Med Genet 28(2):477-81. 1987
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